Coexpression with potassium channel subunits used to clone the Y2 receptor for neuropeptide Y

Mol Pharmacol. 1996 Mar;49(3):387-90.

Abstract

Xenopus oocytes were injected with RNAs for the two inward-rectifier potassium channel subunits Kir3.1 (GIRK1) and Kir3.4 (rcKATP or CIR) in addition to RNA from the neuroblastoma cell line KAN-TS. Potassium currents were evoked by neuropeptide Y in oocytes injected with polyadenylated RNA or with cRNA from pools of a neuroblastoma (KAN-TS) cDNA library, and progressive subdivision of responding pools yielded a single cDNA. The encoded protein contains 381 amino acids, has the seven hydrophobic domains characteristic of G protein-coupled receptors, and is 31% identical to the Y1 receptor: potassium currents were induced by neuropeptide Y (EC50=60pm) and Y2-selective analogues. Coexpression with potassium channel subunits will be a generally useful method for the cloning of G protein-coupled receptors.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • Humans
  • Molecular Sequence Data
  • Neuroblastoma
  • Neuropeptide Y / metabolism*
  • Neuropeptide Y / pharmacology
  • Oocytes / physiology
  • Oocytes / ultrastructure
  • Potassium Channels / genetics*
  • Potassium Channels / metabolism
  • Potassium Channels / physiology
  • RNA / genetics
  • RNA, Messenger / genetics
  • Receptors, Neuropeptide Y / genetics*
  • Receptors, Neuropeptide Y / metabolism
  • Sequence Homology, Amino Acid
  • Tumor Cells, Cultured
  • Xenopus

Substances

  • Neuropeptide Y
  • Potassium Channels
  • RNA, Messenger
  • Receptors, Neuropeptide Y
  • neuropeptide Y2 receptor
  • RNA

Associated data

  • GENBANK/U32500